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Biomedical subjects

B Cinader

Publications and source records attributed to B Cinader.

At least 73 records · Page 4Linked to original sources

T cell antigens and MHC determinants on rabbit granulocytes.

A cell preparation, consisting of 90% granulocytes (polymorphonuclear leukocytes), can be obtained from the rabbit peritoneal cavity. These cells have some membrane antigens, similar to those characteristic of thymus cells (T1, T2), but they do not have the thymus antigen, RTLA. Unlike thymus cells, many polymorphonuclear leukocytes have Ia antigen, in their membranes. Heterogeneity of the cell population is indicated by differences in the number of cells affected by complement-mediated cytotoxic cell-kill with monoclonal antibodies, directed against T1 and T2 and with polyclonal antibodies directed against Ia.

Animals↗

Sensitized spleen B-cells in tolerance-resisting SJL mice.

A subpopulation of B-cells becomes sensitized in the 15-week-old SJL mouse, exposed to aggregate-freed rabbit gamma-globulin, which is highly tolerogenic when given to younger animals. This state of activation can only be expressed in collaboration with sensitized T-cells. The sensitized B-cell does not play an important role in the response of the intact 15-week-old SJL mouse, since there are no sensitized T-cells in the sRGG-treated animals.

Aging↗

Dietary fat alters the fatty acid composition of lymphocyte membranes and the rate at which suppressor capacity is lost.

SJL/J mice were fed from conception two nutritionally adequate semi-purified diets that differed only in polyunsaturated to saturated fatty acid content. The effect of diet fat on the fatty acid composition of membranes from spleen and thymus cells was determined. Diet fat was found to significantly alter the fatty acid composition of lymphocyte membrane phosphatidylcholine and phosphatidylethanolamine. Diet also altered the degree of resistance against tolerance-induction.

Animals↗

Polymorphism of T- and B-cell sensitization by aggregate-freed heterologous gamma-globulin.

Female A/J, C57BL/6J, SJL/J, MRL/MpJ-+/+, MRL/MpJ-lpr/lpr, NZB/BINJ and male BXSB/MpJ mice were injected at various ages with a tolerogenic form of rabbit gamma-globulin, or were left untreated and all were then immunized with dinitrophenylated rabbit gamma-globulin. We could distinguish 4 types of responsiveness to sRGG: (1) persistent T-cell tolerance (A/J, MRL/MpJ-+/+); (2) persistent T-cell tolerance and age-dependent resistance and sensitization of B-cells to tolerance induction (C57BL/6J, NZB/BINJ); (3) decreasing T- and B-cell tolerance (SJL/J, male BXSB/MpJ); and (4) T-cell sensitization in older animals (MRL/MpJ-lpr/lpr). Suppressor capacity and its regeneration was examined in terms of colchicine and cyclophosphamide treatment. Colchicine increased the immune response to a much greater extent in 10-week-old than in 6-week-old MRL/MpJ-lpr/lpr mice and had little effect on MRL/MpJ-+/+ mice. It had a relatively small effect on 15-week-old NZB/B1NJ and a much greater effect on 6-week-old animals. The reason for these differences are discussed.

Aging↗

Aging and the immune system.

Information is presented on changes in the aging immune system. An analysis of separate streams of cellular aging in the inbred mouse is presented. It is demonstrated that there is extensive polymorphism in the aging of different types of executive and regulatory cell lines.

Aging↗

Age-dependent changes in antigenic promotion, a Th-2 type of activity.

Help for a secondary response to a determinant can be dependent on previous exposure to other determinants of the macromolecule; it can also be independent of sensitization to such carrier determinants. A helper effect, which is independent of the hapten carrier bridge, can be seen in the indirect plaque-forming response. This Th-2 type of reactivity was observed in tissue culture with spleen cells from A/J and C57BL/6 mice, immunized with various macromolecules. The spleen cells of these mice were exposed in tissue culture to the sensitizing macromolecule and to antigens conjugated to a macromolecule which was structurally unrelated to the sensitizing macromolecule. Sensitization of the spleen cell donor with the hapten was not required for this help to be given if the hapten was 2,4-dinitrophenyl, but was required when the hapten was p-azobenzene sulfonic acid. The age, at which the Th-2 helper effect was first seen, shows polymorphism. The effect was detected well after sexual maturity, and 50% of the final value was reached only when the animal had passed the 20th week of its life. The variation in age of detectable Th-2 capacity depended on the nature of the hapten; with 2,4-dinitrophenyl, as the hapten, A/J and C57BL/6J differed very little in the age at which the Th-2 capacity became detectable; with p-azobenzene sulfonic acid the Th-2 capacity was detectable at a much later age in A/J than in C57BL/6 mice.

Aging↗

Age-dependent change in a soluble factor responsible for Th-2 type of help in the indirect plaque-forming antibody response.

A carrier-independent type of helper activity for the indirect plaque-forming response was detected in the supernatant of spleen cell suspensions from primed mice. The potency of the factor increased during the adult life of the spleen cell donor. The factor(s) acted antigen nonspecifically and across the major histocompatibility complex. The ability of spleen cells to generate this activity was lost after treatment of primed cells with anti-Thy 1.2, anti-Lyt 1.2, or anti-Ly 7.2, in the presence of complement. The capacity to generate the activity depended on the presence of cells which adhered specifically to surfaces coated with the sensitizing antigen. The production of factor(s) involved cooperation of nonadherent T cells from primed old animals and adherent cells from unprimed donors; the age-dependent change in factor-production did not depend on the age of the donor of adherent cells.

Aging↗

Accelerated development of a Th-2 type factor in animals with and without an imbalance between help and suppression.

A helper factor can be detected in antigen-treated supernatants from spleen T and adherent cells of sensitized animals. This factor promotes an indirect hapten-specific plaque forming response of B cells, irrespective of the identity of the carrier, i.e. provides the Th-2 type of help. Factor production increases with age and occurs most rapidly in strains known to have an accelerated decrease of suppressor capacity. The reason for the inverse correlation between suppressor capacity and the Th-2 type of helper factor is discussed.

Aging↗

The effect of ribavirin and rifamycin SV on age-dependent changes of the immune system during the adult life of SJL mice.

Ribavirin and Rifamycin SV, given from birth to adult life, arrest the loss of suppressor capacity, normally occurring in older SJL mice. The two drugs differ in their effect on Th-2-type help for the indirect plaque-forming response, i.e. for help which is independent of the carrier-hapten bridge. This type of help normally increases with age. Ribavirin treatment inhibits development of Th-2-type of help; Rifamycin SV does not interfere with the development of this type of help. Neither of the two drugs had an effect on the ability of SJL mice, not treated with aggregate-freed RGG, to make a plaque-forming response to aggregated RGG.

Aging↗

A comparison of regulatory cells from rabbit spleen and appendix.

Both spleen and appendix of the rabbit contain two types of accessory cells that regulate the response of T-cells to concanavalin A. These accessory cells are found among non-T, non-B adherent cells and among B-cells. There is, so far, no evidence for a sequential interaction of these two cell types. In addition, there is an inhibitory adherent cell type in the appendix that interferes with the B-cell-regulated proliferative T-cell response.

Animals↗

Rabbit spleen B lymphocytes as helper cells in lymphocyte activation by concanavalin A and phytohaemagglutinin.

Using rosetting methods, we have purified rabbit B cells and studied their interactions with T cells purified by passage over an anti-immunoglobulin-coated Degalan beads column. B cells enhance the response of T cells to concanavalin A (Con A) and phytohaemagglutinin. In regulation of the response to Con A, an adherent cell is a third participating cell. B-cell preparation contain a minority of cells that can respond to T mitogens with the help of non-proliferating T cells, but the proportion of these responding cells is small, and the involvement of the T-cell impurity cannot be excluded.

Animals↗

Mechanisms involved in age-dependent decline of immune responsiveness and apparent resistance against tolerance induction in C57BL/6 mice.

The plaque-forming antibody response of C57BL/6 mice to rabbit gamma globulin (RGG) decreases as a function of ae. RGG in tolerogenic form induces tolerance of young mice but sensitizes older animals. If antigen is administered together with lipopolysaccharide, the age-dependent decline in immune responsiveness is not observed, nor are older animals sensitized by tolerogen. The age-dependent decline in immune responsiveness is due to a loss of T helper capacity; sensitization by tolerogen is attributable to a subpopulation of B cells which becomes sensitized by the tolerogen. Older animals, treated with tolerogen, show a degree of central tolerance of T cells and a relatively slight, age-dependent diminution in colchicine- or cyclophosphamide-sensitive precursors of suppressor cells.

Aging↗

Allotype and charge-related differences in the immune response.

Rabbits homozygous at the Ab kappa chain allotypic locus (Ab4/Ab4 and Ab9/Ab9) were immunized with negatively and positively charged antigens. The negatively charged antigens were bovine serum serum albumin (BSA; pI = 4.9), ovalbumin (OV; pI = 4.9) and two synthetic polypeptides: copolymer L-glutamic acid L-tyrosine (abbreviated TG; pI = 4.8) and multichain poly (L-tyrosine: L-glutamic acid) poly D-alanine: poly L-lysine (poly L-lysine backbone) abbreviated (TG) --AL; pI = 4.8). The positively charged antigen was hen egg lysozyme (LYS; pI = 10.2). Homozygous Ab9 rabbits responding to negatively charged antigens made less antibody than did Ab4 homozygotes. In contrast, both groups of animals responded equally well to positively charged lysozyme. The relative electric charges of the antibodies were assessed by Sephadex A-50 chromatography. The charge distribution was found to depend on the charge of the eliciting antigen. The positively charged antibodies of Ab9/Ab9 rabbits were not nearly as positively charged as those raised in Ab4/Ab4 rabbits. The difference in average electric charges and in the range of these charges between Ig Ab4 and Ig Ab9 explain quantitative differences in antibody formation in response to negatively charged antigens and may be a contributing factor to the "pecking order", i.e. unequal phenotypic expression of light chain genes in Ab4/Ab9 heterozygotes.

Animals↗

Accelerated development of Th-2 type of helper effect in MRL/MpJ-lpr/lpr and BXSB/MpJ mice.

Age-dependent changes, during adult life, in suppressor capacity and B cell responsiveness have been known for some time. In this paper, an age dependent change in helper function, is being reported. A Th-2 type of helper effect can be observed in tissue culture of spleen cells from animals sensitized with a macromolecule. An indirect plaque-forming response to the hapten occurs when the spleen cells are exposed to the sensitizing macromolecule and to the hapten conjugated to a carrier, structurally unrelated to the sensitizing macromolecule. There is considerable polymorphism in the age at which this effect is first demonstrable and at which it reaches mature levels. Mice of inbred stains, with various defects in the suppressor cell circuit (SJL/J, MRL/MpJ-lpr/lpr, BXSB/MpJ show an accelerated development of Th-2 helper capacity in the indirect plaque-forming response.

Aging↗